NDC 75849-200 Valtrum Us Aerobic Sport Immediate Action

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75849-200
Proprietary Name:
Valtrum Us Aerobic Sport Immediate Action
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Laboratorios Quantium Llc
Labeler Code:
75849
Start Marketing Date: [9]
06-06-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75849-200-00

Package Description: 118 g in 1 BOTTLE, SPRAY

Product Details

What is NDC 75849-200?

The NDC code 75849-200 is assigned by the FDA to the product Valtrum Us Aerobic Sport Immediate Action which is product labeled by Laboratorios Quantium Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75849-200-00 118 g in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Valtrum Us Aerobic Sport Immediate Action?

USESFor the temporary relief of minor aches and pains of muscles and joints associated with RheumatismMuscle strainSprainsBruisesNeck and Shoulder Stiffness

Which are Valtrum Us Aerobic Sport Immediate Action UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Valtrum Us Aerobic Sport Immediate Action Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Valtrum Us Aerobic Sport Immediate Action?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1426990 - camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % Topical Spray
  • RxCUI: 1426990 - camphor 25 MG/ML / menthol 25 MG/ML / methyl salicylate 100 MG/ML Topical Spray
  • RxCUI: 1426992 - Valtrum Sport 2.5 % / 2.5 % / 10 % Topical Spray
  • RxCUI: 1426992 - camphor 25 MG/ML / menthol 25 MG/ML / methyl salicylate 100 MG/ML Topical Spray [Valtrum Sport]
  • RxCUI: 1426992 - Valtrum Soothing (camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % ) Topical Spray

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".